ENST00000247933.9:c.1286G>C
|
ENSP00000247933.4:p.Gly429Ala
|
|
ENST00000514224.2:c.1286G>C
MANE Select
|
ENSP00000425081.2:p.Gly429Ala
|
|
ENST00000652070.1:n.1342G>C
|
|
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ENST00000247933.8:c.1286G>C
|
ENSP00000247933.4:p.Gly429Ala
|
|
ENST00000502829.1:n.88G>C
|
|
|
ENST00000514224.1:c.890G>C
|
ENSP00000425081.1:p.Gly297Ala
|
|
ENST00000514698.5:n.1393G>C
|
|
|
NM_000203.4:c.1286G>C
|
NP_000194.2:p.Gly429Ala
|
|
NR_110313.1:n.1374G>C
|
|
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XM_006713882.2:c.890G>C
|
XP_006713945.1:p.Gly297Ala
|
|
XM_011513459.1:c.1352G>C
|
XP_011511761.1:p.Gly451Ala
|
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XM_011513460.1:c.1145G>C
|
XP_011511762.1:p.Gly382Ala
|
|
XM_011513461.1:c.1079G>C
|
XP_011511763.1:p.Gly360Ala
|
|
XM_011513462.1:c.998G>C
|
XP_011511764.1:p.Gly333Ala
|
|
XM_011513463.1:c.998G>C
|
XP_011511765.1:p.Gly333Ala
|
|
XR_924947.1:n.1355G>C
|
|
|
NM_000203.5:c.1286G>C
MANE Select
|
NP_000194.2:p.Gly429Ala
|
|
NM_001363576.1:c.890G>C
|
NP_001350505.1:p.Gly297Ala
|
|
XM_011513461.2:c.1079G>C
|
XP_011511763.1:p.Gly360Ala
|
|
XM_017008163.1:c.326G>C
|
XP_016863652.1:p.Gly109Ala
|
|